Genetic risk factor identification for common epilepsies guided by integrative omics data analysis
In this study, we propose new candidate genes to expand the dataset of potential epilepsy-causing genes. Further research on these genes may enhance our understanding of the complex regulatory mechanisms underlying GGE and other types of epilepsy, potentially revealing targets for therapeutic intervention.
Authors
- Albert J. Becker (ORCID: https://orcid.org/0000-0003-2661-3705)
- Michael Nothnagel (ORCID: https://orcid.org/0000-0001-8305-7114)
- Oluyomi M. Adesoji (ORCID: https://orcid.org/0000-0002-8583-7170)
- Holger Lerche (ORCID: https://orcid.org/0000-0002-1783-8710)
- Herbert Schulz (ORCID: https://orcid.org/0000-0002-0226-964X)
- Patrick May (ORCID: https://orcid.org/0000-0001-8698-3770)
- Roland Krause (ORCID: https://orcid.org/0000-0001-9938-7126)
- Daniela Grimm (ORCID: https://orcid.org/0000-0002-4991-3105)
- Ashwini Mushunuri (ORCID: https://orcid.org/0009-0000-7756-5876)
Institutions
- University of Bonn (DE)
- University of Cologne (DE)
- University of Luxembourg (LU)
- Aarhus University (DK)
- University Hospital Magdeburg (DE)
- Brandenburg University of Applied Sciences (DE)
- University Hospital Cologne (DE)
- University of Tübingen (DE)
- Otto-von-Guericke-Universität Magdeburg (DE)
Publication Details
- Journal
- Epilepsia
- Published
- 2025-11-30
- DOI
- https://doi.org/10.1111/epi.70021
- Primary Topic
- Genetic Associations and Epidemiology
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Deutsche Forschungsgemeinschaft